Portex, Inc. - FDA 510(k) Cleared Devices
20
Total
20
Cleared
0
Denied
Portex, Inc. has 20 FDA 510(k) cleared anesthesiology devices. Based in Walker, US.
Historical record: 20 cleared submissions from 1977 to 2004.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
20 devices
Cleared
Mar 10, 2004
PORTEX 24G PEDIATRIC EPIDURAL AND PERIPHERAL BLOCK ANESTHESIA CATHETER
Anesthesiology
163d
Cleared
Jul 18, 2003
PER-FIT PERCUTANEOUS DILATIONAL TRACHEOSTOMY KIT
Anesthesiology
106d
Cleared
Feb 11, 2003
1ST RESPONSE INTERMEDIATE MANUAL RESUSCITATOR
Anesthesiology
90d
Cleared
Feb 27, 2002
1ST RESPONSE MANUAL RESUSCITATOR, MODEL 85XX
Anesthesiology
75d
Cleared
Feb 13, 2002
HYPODERMIC NEEDLE-PRO INSULIN SYRINE & NEEDLE WITH NEEDLE PROTECTION DEVICE
General Hospital
65d
Cleared
Mar 24, 1988
LARYNGECTOMY TUBE
Ear, Nose, Throat
175d
Cleared
Jan 19, 1988
THERMOVENT 600, 1200, T, 02
Anesthesiology
71d
Cleared
Aug 06, 1986
MINI-TRACH KIT
Anesthesiology
58d
Cleared
Jul 06, 1984
JET VENTILATION ADAPTOR
Cardiovascular
14d
Cleared
Feb 04, 1984
IRRI-CATH
Anesthesiology
82d
Cleared
Jan 17, 1984
ENDOBRONCHIAL TWIN LUMEN TUBE
Anesthesiology
20d
Cleared
Jan 17, 1984
SWIVEL ADAPTOR W/ALARM PORT
Anesthesiology
13d
Cleared
Nov 28, 1983
HYDROFLOW SUCTION IRRIGATION SYSTEM
General & Plastic Surgery
70d
Cleared
Aug 12, 1983
CARDIO-ESOPHASCOPE
Anesthesiology
157d
Cleared
Mar 08, 1983
REINFORCED SILICONE TRACHEAL TUBE
Anesthesiology
33d
Cleared
Feb 05, 1981
ESOPHAGEAL STETHOSCOPE TEMPERATURE PROBE
Anesthesiology
15d
Cleared
Sep 09, 1980
CONTINUOUS EPIDURAL ANESTHESIA TRAY/DRUG
Anesthesiology
13d
Cleared
Nov 20, 1979
TROCAR CATHETER/THORACIC CATHETER
Cardiovascular
18d
Cleared
Aug 02, 1978
CONTINUOUS EPIDURAL ANESTHESIA TRAY
Anesthesiology
41d
Cleared
Mar 14, 1977
SPECIMEN COLLECTOR
General Hospital
54d